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FDA Inspection
•Arcade Marketing Inc.•November 30, 2017

Arcade Marketing Inc. – FDA Inspection, Nov 30, 2017

Record Details

This FDA Inspection record concerns Arcade Marketing Inc., with an inspection on November 30, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Arcade Marketing Inc.
Inspection Date
November 30, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Brandon C. Heitmeier (FDA Associated Person)
View Company Profile

ID · d80ee348-ea69-4b79-ba72-4aba9973d389

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1034466
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.170(b)Annual visual exams of drug products
  2. 21 CFR 211.100(a)Absence of Written Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Arcade Marketing Inc.

2
DateClassificationOfficeProject area
July 20, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 10, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Arcade Marketing Inc.
  • FDA Inspection 1210448 - 2023-07-20
  • FDA Inspection 776516 - 2012-04-10

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